117 related articles for article (PubMed ID: 10798187)
1. [Pair of siblings of Italian ethnicity with hyperferritinemia and cataract].
Volkmann M; Schiff JH; Hör M; Hentze MW; Fiehn W; Merkt J
Internist (Berl); 2000 Apr; 41(4):381-4. PubMed ID: 10798187
[No Abstract] [Full Text] [Related]
2. Hereditary hyperferritinemia-cataract syndrome: a novel mutation in the iron-responsive element of the L-ferritin gene in a French family.
Garderet L; Hermelin B; Gorin NC; Rosmorduc O
Am J Med; 2004 Jul; 117(2):138-9. PubMed ID: 15234655
[No Abstract] [Full Text] [Related]
3. Hereditary hyperferritinemia cataract syndrome: a de novo mutation in the iron responsive element of the L-ferritin gene.
Arosio C; Fossati L; Viganò M; Trombini P; Cazzaniga G; Piperno A
Haematologica; 1999 Jun; 84(6):560-1. PubMed ID: 10366804
[No Abstract] [Full Text] [Related]
4. A point mutation in the iron-responsive element of the L-ferritin in a family with hereditary hyperferritinemia cataract syndrome.
Wong K; Barbin Y; Chakrabarti S; Adams P
Can J Gastroenterol; 2005 Apr; 19(4):253-5. PubMed ID: 15861269
[TBL] [Abstract][Full Text] [Related]
5. Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndrome.
Barton JC; Beutler E; Gelbart T
Blood; 1998 Dec; 92(11):4480. PubMed ID: 9882097
[No Abstract] [Full Text] [Related]
6. Dual diagnoses of hereditary hyperferritinaemia-cataract syndrome and hereditary haemochromatosis.
Hughes M; Vosylius P
Clin Lab Haematol; 2006 Oct; 28(5):357-9. PubMed ID: 16999731
[TBL] [Abstract][Full Text] [Related]
7. A point mutation in the bulge of the iron-responsive element of the L ferritin gene in two families with the hereditary hyperferritinemia-cataract syndrome.
Martin ME; Fargion S; Brissot P; Pellat B; Beaumont C
Blood; 1998 Jan; 91(1):319-23. PubMed ID: 9414300
[TBL] [Abstract][Full Text] [Related]
8. Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation").
Girelli D; Corrocher R; Bisceglia L; Olivieri O; De Franceschi L; Zelante L; Gasparini P
Blood; 1995 Dec; 86(11):4050-3. PubMed ID: 7492760
[TBL] [Abstract][Full Text] [Related]
9. Description of a new mutation in the L-ferrin iron-responsive element associated with hereditary hyperferritinemia-cataract syndrome in a Spanish family.
Balas A; Aviles MJ; Garcia-Sanchez F; Vicario JL
Blood; 1999 Jun; 93(11):4020-1. PubMed ID: 10383191
[No Abstract] [Full Text] [Related]
10. [Hereditary hyperferritinemia-cataract syndrome].
Merkt J
Dtsch Med Wochenschr; 1997 Apr; 122(16):504-6. PubMed ID: 9162623
[TBL] [Abstract][Full Text] [Related]
11. [Molecular genetics of hereditary cataract-hyperferritinemia syndrome].
Milon B; Beaumont C
Ann Biol Clin (Paris); 1998 Jul; 56 Spec No():36-40. PubMed ID: 9827213
[No Abstract] [Full Text] [Related]
12. Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome.
Cicilano M; Zecchina G; Roetto A; Bosio S; Infelise V; Stefani S; Mazza U; Camaschella C
Haematologica; 1999 Jun; 84(6):489-92. PubMed ID: 10366790
[TBL] [Abstract][Full Text] [Related]
13. Two Dutch families with hereditary hyperferritinaemia-cataract syndrome and heterozygosity for an HFE-related haemochromatosis gene mutation.
Simsek S; Nanayakkara PW; Keek JM; Faber LM; Bruin KF; Pals G
Neth J Med; 2003 Sep; 61(9):291-5. PubMed ID: 14692443
[TBL] [Abstract][Full Text] [Related]
14. [Hereditary hyperferritinemia and cataract syndrome: a de novo mutation].
Hernández Martín D; Cervera Bravo A; Balas Pérez A
An Pediatr (Barc); 2008 Apr; 68(4):408-10. PubMed ID: 18394394
[No Abstract] [Full Text] [Related]
15. Double-gradient denaturing gradient gel electrophoresis assay for identification of L-ferritin iron-responsive element mutations responsible for hereditary hyperferritinemia-cataract syndrome: identification of the new mutation C14G.
Cremonesi L; Fumagalli A; Soriani N; Ferrari M; Levi S; Belloli S; Ruggeri G; Arosio P
Clin Chem; 2001 Mar; 47(3):491-7. PubMed ID: 11238302
[TBL] [Abstract][Full Text] [Related]
16. Identification of a novel mutation in the L ferritin iron-responsive element causing hereditary hyperferritinemia-cataract syndrome.
Messa E; Pellegrino RM; Palmieri A; Carturan S; Cilloni D; Saglio G; Roetto A
Acta Haematol; 2009; 122(4):223-5. PubMed ID: 19887780
[No Abstract] [Full Text] [Related]
17. [Hereditary hyperferritinemia cataracts syndrome in a Spanish family caused by the A40G mutation (Paris) in the L-ferritin (FTL) gene associated with the mutation H63D in the HFE gene].
Del Castillo Rueda A; Fernández Ruano ML
Med Clin (Barc); 2007 Sep; 129(11):414-7. PubMed ID: 17927936
[TBL] [Abstract][Full Text] [Related]
18. Gene symbol: FTL. Disease: Hyperferritinemia-cataract syndrome.
Piperno A; Pelucchi S
Hum Genet; 2004 Mar; 114(4):406. PubMed ID: 15046083
[No Abstract] [Full Text] [Related]
19. [Hereditary hyperferritinaemia-cataract syndrome].
Simsek S; Nanayakkara PW
Ned Tijdschr Geneeskd; 2003 Dec; 147(51):2557; author reply 2557-8. PubMed ID: 14735856
[No Abstract] [Full Text] [Related]
20. A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome.
Aguilar-Martinez P; Biron C; Masmejean C; Jeanjean P; Schved JF
Blood; 1996 Sep; 88(5):1895. PubMed ID: 8781450
[No Abstract] [Full Text] [Related]
[Next] [New Search]